ENST00000436784.7:c.*5A>C
MANE Select
|
ENSP00000389175.2:n.*5A>C
|
|
ENST00000436784.6:c.*5A>C
|
ENSP00000389175.2:n.*5A>C
|
|
ENST00000461183.5:c.849A>C
|
ENSP00000417264.1:p.Ala283=
|
|
ENST00000471180.5:c.720A>C
|
ENSP00000417526.1:p.Ala240=
|
|
ENST00000473032.5:c.615A>C
|
ENSP00000418951.1:p.Ala205=
|
|
ENST00000486393.5:c.*940A>C
|
ENSP00000419868.1:n.*940A>C
|
|
ENST00000489173.1:n.1871A>C
|
|
|
NM_145262.3:c.*5A>C
|
NP_660305.2:n.*5A>C
|
|
NR_026699.1:n.1675A>C
|
|
|
NR_026700.1:n.781A>C
|
|
|
NR_026701.1:n.1673A>C
|
|
|
NR_026702.1:n.711A>C
|
|
|
XM_005264878.2:c.*696A>C
|
XP_005264935.1:n.*696A>C
|
|
XR_245095.2:n.2828A>C
|
|
|
XM_017005730.1:c.*5A>C
|
XP_016861219.1:n.*5A>C
|
|
XM_024453351.1:c.*5A>C
|
XP_024309119.1:n.*5A>C
|
|
XM_024453352.1:c.*696A>C
|
XP_024309120.1:n.*696A>C
|
|
XR_001740022.2:n.3479A>C
|
|
|
XR_001740023.2:n.3003A>C
|
|
|
XR_245095.4:n.2829A>C
|
|
|
NM_145262.4:c.*5A>C
MANE Select
|
NP_660305.2:n.*5A>C
|
|
NR_026699.2:n.1667A>C
|
|
|
NR_026700.2:n.773A>C
|
|
|
NR_026701.2:n.1665A>C
|
|
|
NR_026702.2:n.703A>C
|
|
|
NM_001144951.2:c.*696A>C
|
NP_001138423.1:n.*696A>C
|
|